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Fluorescence properties of curcumin-loaded nanoparticles for cell tracking
Authors Mogharbel BF , Francisco JC , Irioda AC, Dziedzic DSM , Ferreira PE, Souza D , Souza CMCO, Bergonse Neto N , Guarita-Souza LC , Franco CRC, Nakamura CV, Kaplum V, Mazzarino L, Lemos-Senna E , Borsali R, Soto PA, Setton-Avruj P, Abdelwahid E, Carvalho KA
Received 14 April 2018
Accepted for publication 30 May 2018
Published 28 September 2018 Volume 2018:13 Pages 5823—5836
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Dr Thomas J Webster
Bassam Felipe Mogharbel,1 Julio Cesar Francisco,1 Ana Carolina Irioda,1 Dilcele Silva Moreira Dziedzic,1 Priscila Elias Ferreira,1 Daiany de Souza,1 Carolina Maria Costa de Oliveira Souza,1 Nelson Bergonse Neto,2 Luiz Cesar Guarita-Souza,2 Celia Regina Cavichiolo Franco,3 Celso Vataru Nakamura,4 Vanessa Kaplum,4 Letícia Mazzarino,5 Elenara Lemos-Senna,6 Redouane Borsali,7 Paula A Soto,8 Patricia Setton-Avruj,8 Eltyeb Abdelwahid,9 Katherine Athayde Teixeira de Carvalho1
1Cell Therapy and Biotechnology in Regenerative Medicine Department, Pelé Pequeno Príncipe Institute, Child and Adolescent Health Research and Pequeno Príncipe Faculty, Curitiba, Paraná, Brazil; 2Institute of Biological and Health Sciences, Pontifical Catholic University of Paraná (PUCPR), Centro de Ciências Biológicas e da Saúde (CCBS), Curitiba, Brazil; 3Cell Biology Department, Federal University of Paraná, Curitiba, Paraná, Brazil; 4Department of Pharmaceutical Sciences, Universidade Estadual de Maringá, Maringá, Paraná, Brazil; 5Department of Pharmaceutical Sciences, NanoBioMat Laboratory, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil; 6Department of Pharmaceutical Sciences, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil; 7Centre de Recherches sur les Macromolécules Végétales (CERMAV), Centre National de la Recherche Scientifique (CNRS), University Grenoble Alpes, F-38000, Grenoble, France; 8Instituto de Química y Físicoquímica Biológica (IQUIFIB), Departament of Química Biológica, Facultad de Farmacia y Bíoquímica, Universidad de Buenos Aires (UBA) Consejo nacional de Investigaciones Científicas y Técnicas (CONICET), Buenos Aires, Argentine; 9Feinberg School of Medicine, Feinberg Cardiovascular Research Institute, Northwestern University, Chicago, Il, USA
Background: Posttransplant cell tracking, via stem cell labeling, is a crucial strategy for monitoring and maximizing benefits of cell-based therapies. The structures and functionalities of polysaccharides, proteins, and lipids allow their utilization in nanotechnology systems.
Materials and methods: In the present study, we analyzed the potential benefit of curcumin-loaded nanoparticles (NPC) using Vero cells (in vitro) and NPC-labeled adipose-derived mesenchymal stem cells (NPC-ADMSCs) (in vivo) in myocardial infarction and sciatic nerve crush preclinical models. Thereafter, transplantation, histological examination, real time imaging, and assessment of tissue regeneration were done.
Results: Transplanted NPC-ADMSCs were clearly identified and revealed potential benefit when used in cell tracking.
Conclusion: This approach may have broad applications in modeling labeled transplanted cells and in developing improved stem cell therapeutic strategies.
Keywords: mesenchymal stem cells, transplantation, cell marking, myocardium infarction, sciatic nerve crush
Regenerative medicine has the objective to restore the lost functions of an organ or tissue1 and has been searching for newer alternatives for posttransplant cell tracking in cell-based therapies. Thus, stem cell labeling is a crucial aim in research, since the techniques that are usually used are invasive or contrast dependent.2 Materials used for this purpose include quantum dots, carbon nanotubes, and nanoparticles containing both inorganic elements such as iron, silver, copper, and zinc oxide and synthetic or biological elements. Markers in this context vary in size, material, antigenicity, and degradability, although all of them need to ensure tolerance and avoid side effects.3–6
In such scenario, biopolymers emerge as a promising technique. The structures and functional properties of polysaccharides, proteins, and lipids allow their utilization in nanotechnology systems.7,8 In particular, curcumin properties and its fluorescence have been widely described in the literature.9–11
Curcumin has been used in several studies and shown therapeutic promises, particularly its anti-oxidant and anti-cancer properties.12,13 In addition, curcumin can enhance adipose-derived mesenchymal stem cell (ADMSC) survival after transplantations, mostly through heme oxygenase-1 expression, which prevents cell death caused by oxidative stress.14,15 Interestingly, ADMSC pretreated with curcumin displayed improved myocardial recovery through an increase in vascular endothelial growth factor production, enhanced antiapoptotic ability, stimulation of neovascularization in peri-infarcted area, and reduced infarct size.16 However, its fluorescence properties as an imaging probe are not utilized as described in this study.
On the other hand, extensive clinical trials using stem cells, particularly in the treatment of onco-hematological diseases, opened up the possibility of evaluating stem cells for treatment of non-hematopoetic affections. Mesenchymal stem cells (MSCs) represent a promising source for regeneration and repair of various tissues, due to their presence in adult solid organs as well as in the mesoderm of embryonic tissue.17,18 In this study, we investigated the fluorescence properties of curcumin-loaded nanoparticles for tracking cellular therapy.
Materials and methods
The experimental design is presented in Figure 1.
Figure 1 Diagram for in vitro and in vivo studies.
In vitro studies
Preparation and characterization of nanoparticles
Unloaded polycaprolactone nanoparticles (NP) and curcumin-loaded polycaprolactone nanoparticles (NPC) were prepared using the nanoprecipitation method as previously described by Mazzarino et al.19 Particle size and zeta potential were detected by dynamic light scattering (DLS) and laser-doppler anemometry, respectively, using a Zetasizer Nano Series (Malvern Instruments, Worcestershire, UK). Curcumin was determined using a UV/Vis spectrophotometric method.20 The total concentration of curcumin in the nanoparticle suspensions was measured after their complete dissolution in acetonitrile. Encapsulation efficiency was calculated by the difference between the total concentration of curcumin found in the nanoparticle suspensions and the concentration of the free drug in the ultrafiltrate obtained after the separation of nanoparticles by ultrafiltration/centrifugation.
Nanoparticle flow cytometric analysis
Flow cytometric analysis using 488 nm blue laser was made to confirm the emission wavelength of the NPC using the cytometer FACS Canto II (Becton Dickinson Biosciences, Franklin Lakes, NJ, USA). The NPCs were suspended in PBS (Sigma-Aldrich Co., St Louis, MO, USA) to obtain a final concentration of 10 μM and 1 mL of volume. In addition, a 1 mL suspension of NP was prepared. The data were analyzed with Infinicyt software (Cytognos S.L., Santa Marta de Tormes, Salamanca, Spain).
Scanning electronic microscopy
The used Vero cells (CCL-81, TECPAR) were approved by institutional committee for laboratory animal control, number: 025–12 01 2014 of CEUA-Complexo Hospitalar Pequeno Príncipe (Curitiba, Brazil). Vero cells were seeded in wells with cover slips until reaching 80% of confluence. At this point, the culture medium was replaced with a fresh culture medium containing 30 μM NPC. The wells were washed with 0.1M sodium cacodylate buffer, pH 7.4 at 4°C. The cells were then fixed in Karnovski solution (2% gluteraldehyde, 4% paraformaldehyde, 1 mM calcium chloride [CaCl2] in 0.1M cacodylate buffer, pH 7.2–7.4) for an hour, and then washed three times in 0.1M sodium cacodylate buffer, pH 7.4. Then the cells were dehydrated with crescent ethanol concentrations (30%, 50%, 70%, 90%, and 100% twice) for 10 minutes at each concentration. Afterward, the critical point and gold coating were obtained using the equipment (CPD-Balzers Union/Baltec, Germany) for (CPD 030 BALTEC, Pfäffikon, Switzerland). The cells were then analyzed with scanning electron microscopy (SEM) (Vega-3LMU; Tescan, Brno, Kahoutovice-Czec Republic).
The cytotoxicity was evaluated by using the MTT assay. These NPC were cultured in DMEM-High Glucose (Sigma-Aldrich Co.) containing 10% fetal bovine serum (Thermo Fisher Scientific, Waltham, MA, USA), 1% penicillin (100 U/mL) and streptomycin (100 μg/mL) (Thermo Fisher Scientific) and incubated at 37°C and 5% CO2. For the MTT assay, cells were seeded in a 24-well plate (1 × 104 cells/cm2) in media containing 30 μM concentration of NPC and incubated at 37°C for 24 hours. After incubation, the cells were washed with PBS, the medium was changed, and MTT solution (Sigma-Aldrich Co.) was added and incubated for 3 hours at 37°C. Subsequently, cells were washed to remove the supernatant, and 100 μL of dimethyl sulfoxide (Sigma-Aldrich Co.) was added. The cells were then shaken for 5 minutes, and the absorbance was measured at 595 nm on a microplate reader (EL800; Biotek Instruments Inc., Winooski, VT, USA).
Statistical analysis was done by using the one-way ANOVA test. P-values <0.05 were considered to be significant and calculated using the Graph-Pad Prism (GraphPad Software Inc., La Jolla, CA, USA) software. The graph shows 95% CI of the mean ± SD.
In vitro fluorescence identification
Vero cells were seeded on 96-well plates (1 × 104 cells/cm2) and treated with 30 μM NPC for 72 hours at 37°C. After incubation, cells were washed with PBS and new culture medium was added. The cells were evaluated for 24 days, with medium changed every 2 days. Images were captured using a fluorescence microscope (Axio Vert.A1; Carl Zeiss Meditec AG, Jena, Germany).
ADMSC isolation, culture, and incubation with NPCs for transplantation
The cells were isolated from inguinal fat of Wistar rats by enzymatic dissociation with the aid of Collagenase IA (Sigma-Aldrich Co.). Cells were cultured in DMEM F12 (Sigma-Aldrich Co.) containing 10% fetal bovine serum (Thermo Fisher Scientific), penicillin (100 U/mL), and streptomycin (100 μg/mL) (Sigma-Aldrich Co.) at 37°C and 5% CO2. Cells were then seeded in 24-well plates (1 × 105 cells/cm2) and incubated for 72 hours with NPC at 37°C. After incubation, cells were washed with PBS for supernatant removal. Images were captured using a fluorescence microscope to demonstrate the fluorescence of NPCs in cultured ADMSC.
On the other hand, and following incubation with NPC, another group of cells was washed with PBS and treated with 100 μL of trypsin (Thermo Fisher Scientific) for 5 minutes at 37°C. Cells were then added to culture medium containing fetal bovine serum to stop trypsin action and were subjected to centrifugation for 5 minutes at 1,400 rpm. The supernatant was discarded and the cells were suspended in 25 μL of culture medium for transplantation.
Cell flow cytometric analysis
The immunophenotyping of the cells was done with the flow cytometric apparatus FACS Canto II (Becton Dickinson Biosciences) and using cell membrane markers: CD34 (phycoerythrin [PE]), CD45 (PerCP-Cy5-5), CD73 (fluroscein isothiocyanate [FITC]), and CD90 (PE-CY7) (Becton Dickinson Bioscience). The following isotype negative controls were used: FITC Mouse IgG1 κ, PE Mouse IgG2a κ, PE-Cy7 Mouse IgG1 κ, PERCP Mouse IgG1 κ (Becton Dickinson Bioscience).
A fraction of the cells were transferred to two cytometry tubes containing 100 μL of PBS and incubated for 15 minutes in a dark room with the cell membrane markers as well as with the isotype controls. After incubation, the tubes were washed with PBS and then centrifuged for 5 minutes at 1,400 rpm. The cells were suspended with PBS and analyzed by the flow cytometer.
In vivo studies
All rats were kept under standard conditions with food and water ad libitum on a 12-hour day/night cycle (light on at 7:00 am). All animals were euthanized with a lethal dose of pentobarbital sodium (thiopental) 200–250 mg/kg intraperitoneally (IP).
The protocol of myocardial and in vivo analysis studies was approved by each institutional committee for laboratory animal control (number: 025–12 01 2014 of CEUA – Complexo Hospitalar Pequeno Príncipe [Curitiba, Brazil]) and for crush studies (number: 0040963/2015 of CUDAP: EXP-UBA, Facultad de Farmacia y Bioquímica Universidade de Buenos Aires [Buenos Aires, Argentina]) in accordance with the guidelines for the care and use of laboratory animals published by ARRIVE and the US National Institutes of Health.21
In vivo fluorescence identification
Anesthetized animals were placed in the Carestream in vivo MS FX-Pro (Bruker Corporation, Billerica, MA, USA) for quantification of the baseline. Then the abdominal region was divided in four quadrants and each one was injected with 200 μL of a different solution. The four solutions injected were NP-ADMSC, NPC-ADMSC, NP, and NPC. The region of interest was excited at 480 nm and the emission wavelength was 535 nm.
Fluorescence and histological analysis
NPC-labeled ADMSC were subcutaneously injected in Wistar rats subjected to different experimental conditions and then analyzed for fluorescence detection and histological studies.
Myocardial infarction model
Adult male Wistar rats (70 days old, 270–300 g body weight) (n=4) were anesthetized with ketamine (75 mg/kg IP) and xylazine (10 mg/kg IP). Each animal was submitted to a trichotomy on the left ventrolateral portion of the chest, immediately before the surgical procedure. The animal was positioned in supine with a slight tilt to the right, thus facilitating the exposure of the area to be approached. Rats were then subjected to orotracheal intubation and left thoracotomy in the third intercostal space, following antisepsis in chest. After opening the left pleura, the pericardium was exposed and the heart visualized. Subsequently, the left coronary artery was ligated with polypropylene nonabsorbable monofilament suture 4.0. The infarcted area was immediately identified by heart color changes. Afterward, the heart was replaced in the chest; the hyperinflated lungs and the chest wall were sutured layer by layer using mononylon sutures (nonabsorbable 3.0). After recovery from anesthesia, the animals were kept in cages with water and food ad libtum (Figure S1).
ADMSC labeled with NPC transplantation in myocardial infarction
One week after surgeries, the animals were anesthetized, left lateral thoracotomy was performed, and the heart was exposed, prepared, and analyzed.
The NPC-labeled ADMSC were injected into the transition area of the posterior wall of the left ventricle, and the infusion of 25 μL of cell solution was done at a concentration of 5 × 105 cells/mL using Hamilton syringe (702RN; Hamilton Company, Reno, NV, USA) (Figure S2).
The euthanasia was done at 1 week after transplantation of MSC containing the NPC, and the hearts were collected for histological analysis. The hearts were immediately frozen in liquid nitrogen and the sections (8–10 μm thick) were obtained using a cryostat microtome (Leica Biosystems Nussloch GmbH, Nussloch, Germany) at −20°C.
Some of the sections were stained with H&E to evaluate myocardial morphology and the cross-sections allowed us to evaluate all heart layers, including the infarcted region, where NPC-labeled ADMSC would be found; other sections were incubated at room temperature with Hoechst 33258 (Thermo Fisher Scientific) for the nuclei stain (0.2 μg/mL), and images were captured using a fluorescence microscope (Axio Vert.A1; Carls Zeiss).
Sciatic nerve crush
Male and female Wistar rats (70 days old, 270–300 g body weight) were anesthetized with ketamine (75 mg/kg IP) and xylazine (10 mg/kg IP). Their right sciatic nerves were then exposed at mid-thigh level by dissecting an 8–10 mm long segment from the surrounding tissue and crushed for 8 seconds with jeweler’s forceps (N°5 Dumont forceps) as previously described.22 After 7 days, both sciatic nerves were carefully dissected out; the proximal, crush, and distal areas in the right nerve (ipsilateral) and the left nerve (contralateral) were identified.
Injection of isolated ADMSC
ADMSCs were isolated from two male rats. Immediately after crush, an intravascular injection of 200 μL of media containing 3 × 106 NPC-labeled ADMSC was done through the sacra media artery using a 21-gauge hypodermic needle.
In parallel, as a positive control for fluorescent cells, a group of animals received a transplant of ADMSC labeled with the cell tracker orange CMTMR (5-(and 6)-(((4-chloromethyl) benzoyl) amino) tetramethyl-rhodamine) (Thermo Fisher Scientific Inc). For this purpose, the pellet containing the cells was suspended in α-Modified Eagle Medium (MEM) (Thermo Fisher Scientific) with the cell tracker and incubated for 45 minutes at 37°C under sterile conditions. Then the probe solution was replaced with fresh medium and the cells were incubated for 30 minutes. Two animals were used for each group of study: CMTMR, NPC, Sham, in total it was six animals.
Seven days post-crush, the animals were perfused as described previously by Usach et al.22 The presence of NPC- and CMTMR-labeled ADMSC in the control and crushed sciatic nerves was evaluated in cryostat sections using fluorescence microscopy (Axio Vert.A1; Carls Zeiss).
In vitro studies
The main physicochemical properties of nanoparticle suspensions used in this study are summarized in Table 1. According to DLS measurements, NP and NPC had a mean diameter of 194.9 nm and 189.4 nm, respectively, and monodisperse size distribution (polydispersity index <0.2). Finally, nanoparticles showed a curcumin content of about 426.0 μg/mL and encapsulation efficiency values higher than 99%, demonstrating their suitability in the encapsulation of this compound.
Table 1 Physicochemical properties of unloaded (NP) and curcumin-loaded (NPC) nanoparticles
Immunocytochemistry analyses of NPC demonstrated fluorescence emission wavelength for FITC (519 nm), PE (578 nm), and PerCP (678 nm) (Figure 2). FITC and PE have emission wavelength near green fluorescent protein (511 nm), which was used in fluorescence microscopy (Figure 3).
Figure 2 NPC and NP flow cytometry showing the fluorescence of NPC.
The analysis was done during 24 consecutive days, and the fluorescence detected in Vero cells identified with NPC was the highest in the first 8 days (Figure 3).
Cell cytometric analysis
The cytometric analysis demonstrated that cells from adipose tissue were mesenchymal stems cells evidenced by their immunophenotypic profile based on ISHAGE guidelines23 (Figure 4).
SEM analysis demonstrated NPC tendency to cluster and attach to the cell membrane before being internalized (Figure 5). Images of control cells available shown in Figure S3.
Cytotoxicity analysis demonstrated that NPC at a concentration of 30 μM were not significantly toxic to Vero cells (Figure 6).
Figure 6 MTT assay showing no significant differences (P=0.8575) between the studied groups (one-way ANOVA statistical test).
In vivo studies
In vivo fluorescence identification
Upon performing in vivo analysis by Carestream in vivo MS FX-Pro (Bruker Corporation, Billerica, MA, USA), the fluorescence signal was demonstrated only in the quadrant that received the NPCs without cells (Figure 7).
The myocardial infarction model was made according to the steps described earlier (Figure S1). Infarction area was demonstrated by the change of color of the myocardial tissue after left coronary ligation (Figure S4). NPC-ADMSC transplant was done by epicardial injections 1 week after myocardial infarction (Figure S5). NPC were identified in myocardial tissue 1 week after transplantation (Figure 8). The choice of euthanasia after 1 week was based on fluorescence results in vitro.
Sciatic nerve crush
NPC labeling of ADMSC in the ipsilateral sciatic nerve 7 days post-injury and transplantation (Figure 9) was detected by confocal microscopy.
In vitro studies
After DLS measurements of NP and NPC mean diameter and distribution, those values of zeta potential (Table 1) were close to neutral due to the layer of nonionic surfactant poloxamer. With regard to the nanoparticle suspensions used, their high encapsulation efficiency is probably related to the poor water solubility of curcumin in external phase. Flow cytometric analyses of NPC was demonstrated on three fluorescence emission channels with wavelength for FITC (519 nm), PE (578 nm), and PerCP (678 nm), and the fluorescence detection in Vero cells containing NPC in their cytoplasm was the highest in the first 8 days. These were the first steps to establish the study to investigate the fluorescence properties of curcumin-loaded nanoparticles for tracking cellular therapy.
The cell cytometric analysis was confirmed by assessing the phenotype markers CD73+/CD90+/CD45−/CD34; the cells had successful trilineage differentiation (data not shown).23 We did not use the CD105 cell membrane marker. This limitation, however, did not disturb the main objective of this study, which consists in the identification of the cells posttransplant without a therapeutic aim, and only involves simulation. This study did not analyze the function of myocardial infarction neither the sciatic nerve after transplantation.
As demonstrated with the SEM images, the NPC was along the cell surface; nevertheless, the mechanisms of their internalization remain unknown, although similar nanoparticles have been found to accumulate in endosomes described by Ucisik et al.24
The cytotoxicity analysis finding is certainly advantageous for research using NPC in cell transplantation. Our results are supported by the fact that curcumin is well known for its medical uses and low toxicity even in higher concentrations.25 In addition, both curcumin and polycaprolactone are biodegradable and appear to be biocompatible with human health.24,26
In vivo studies
The in vivo fluorescence identification suggested that the analysis with the equipment requires higher concentrations of NPCs so that the fluorescence can be detected. The absence of the fluorescence identification at the regions that were injected with NPC-ADMSC can be explained by the fact that the cells cannot store all NPCs that were incubated with them, ie, the amount of NPCs exceeds the maximum uptake ability of the cells.
The myocardial infarction model using transplanted NPC-ADMSC in myocardial tissue was in accordance with earlier studies that revealed decreased number of surviving cells after the first week of transplantation when their effects are mostly paracrine.27–29 Thus, our strategy is feasible and does not require additional manipulation by survival enhancing strategies.30
The sciatic nerve crush model using transplanted NPC-ADMSC was made 7 days post-injury; this survival time was selected because it corresponds to the peak of demyelination and because when transplanted, CMTMR-labeled ADMSC were exclusively recruited in the ipsilateral nerve.22 The results obtained demonstrate that NPC-labeled ADMSC also migrate exclusively to the demyelinated area of the ipsilateral nerve, ie, distal areas.
Furthermore, it is interesting to emphasize that this was the first study to demonstrate that biopolymer nanoparticles could be used for cell tracking in cell-based therapy, whereas the other authors proposed inorganic nanoparticles.31,32
Our in vivo and in vitro studies identified that transplanted NPC cells, by histological/fluorescence analysis, revealed the benefit of their potential use in cell tracking. In addition, it was possible to analyze cell integration by examining various biopsies.
Although further studies may be necessary to improve fluorescence methodology and ensure safety, these findings suggest a promising strategy for using NPC as markers for stem cell tracking and constitute a step forward in cell therapy applications.
We would like to thank financial support of Institut Carnot POLYNAT (France), CERMAV (France), Luciana Lopes from Instituto de Tecnologia do Paraná (TECPAR) (Brazil) for the Vero cell line supply, and Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) (Brazil).
The authors report no conflicts of interest in this work.
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Figure S1 Illustration showing localization of the left coronary artery (A) and the steps of ligation of the left coronary artery (B–D).
Figure S3 (A and B) Control Vero cells at 3,500× and 25,000×, respectively (SEM).
Figure S4 (A) Heart exposition of the coronary artery. (B–D) Ligation of the left coronary artery.
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